Antifungal antibiotic a 9145 and process for production thereof

ABSTRACT

Antibiotic A-9145 produced by culturing Streptomyces griseolus NRRL 3739 in a nutrient culture medium under submerged aerobic fermentation conditions is recovered therefrom and obtained as a white amorphous water-soluble powder. Antibiotic A-9145 forms acid addition salts with pharmaceutically acceptable acids and inhibits growth of bacteria and fungi, especially Candida albicans.

United States Patent 1 Hamill et al.

[111 3,758,681 451 Sept. 11,1973

ANTIFUNGAL ANTlBlOTlC A-9l45 AND PROCESS FOR PRODUCTION THEREOF Inventors: Robert L. Hamill, New Ross; Marvin M. Hoehn, Indianapolis, both of lnd.

Assignee: Eli Lilly and Company, Indianapolis,

Ind.

Filed: May 22, 1972 Appl. No.: 255,864

Related U.S. Application Data Continuation-impart of Ser. No, 57,438, July 23, 1970, abandoned.

U.S. Cl. 424/118, 195/80 Int. Cl A61k 21/00 [58] Field of Search 424/118; 195/80 Primqry Examiner lerg'ne D Goldberg Attorney Everet l S mithJWiIliam BJ Scanlon et a].

[5 7 ABSTRACT 3 Claims, 1 Drawing Figure Patented Sept. 11,1973

00h 0m 00m O8 0880009 00: OOQOOQOOSOOQ v ATEUV UZwDGmmL mim 955.54% 558% 205x82 5552 ANTIFUNGAL ANTIBIOTIC A 9l45 AND PROCESS FOR PRODUCTION THEREOF CROSS-REFERENCE o RELATEDAPPLlCATlON This application is a continuation-in-part application of US. Pat. application Ser. No. 57,438, filed July 23, 1970, now abandoned.

SUMMARY This invention relates to a novel antibiotic and to a method for its production. In particular this invention relates to a basic, nitrogenous antibiotic having valuditions. The fermentation is carried outat a tempera-' ture of about 30 C. for about 2 to 4 days during which substantial antibiotic activity is produced.

The antibiotic A-9l45 is recovered from the fermentation medium and isolated suitably by adsorption on a cationic exchange resin and elution therefrom with a dilute mineral acid. The antibiotic can be purified by chromatography over a nonionic adsorbent such as carbon or cellulose and obtained as a water-soluble white amorphous powder. With pharmaceutically acceptable acids, it forms salts such as the acid addition salts formed with hydrochloric acid, sulfuric acid and other inorganic acids and the acid addition salts formed with organic acids such as the acetate, maleate, citrate and the like. I

The antibiotic and the acid addition salts thereof inhibit the growth of microorganisms which are pathogenie to animal and plant life. In particular A-9145 inhibits the growth of a variety of fungi and is especially useful in inhibiting the growth of Candida al bicans both in vitro and in vivo.

DETAILED DESCRIPTION Antibiotic A-9145 is a white amorphous powder, highly soluble in water and substantially insoluble in methanol, ethanol, the higher alcoholsand most common organic solvents. Elemental analysis of a smap'le of A-9145 gives the following approximate percentage composition: C, 46.47; H, 6.8; N, 22.28; 0, 26.22

Electrometric titration of a sample of the antibiotic dissolved in 66 percent aqueous dimethylformamide shows the presence of four titratable groups having pKa values of 2.9, 3.9, 8.9 and- 10.2. The apparent molecular weight as calculated from the titration data is approximately 510. I v

The infrared absorption spectrum of A-9145 in a mineral oil mull is shown in the accompanying drawing and contains absorption maxima at the following observed values over the range of 2.5 to l-3.0.microns: 3.0, 3.15, 5.85, 6.00, 6.02, 6.07, 6.22, 6.30, 6.74,6.83, 7.07, 7.26, 7.32, 7.52, 7.69, 8.01, 8.27,'8.88 9.2, 9.57, 11.0, 11.8 and 12.56. v The ultraviolet absorption spectrum of A-9 145, in an aqueous solution containing 0.170'mg. of A-9 145 in 10 m1. of water shows the following absorption maxima at the indicated pH:

neutral pH 206 mp, E,,.,,,"* 520 258 mu, E,,,. 325 acidic pH 7 256 mu, E 325 basic pH 258 lnm 325 Antibiotic A-9145 isa basic substance which is absorbed on the acidic resins, for example, the cationic exchange resins of the IRC 50 type.

A-9145 reacts with acetic anhydride to form multiple acetylderivatives. For example, A-9145 reacts with acetic anhydride in methanol at room temperature to form an acetylated product containing approximately three acetyl groups pr molecule. When A-9l45 is reacted with acetic anhydride in-pyridine at room temperature, the reaction product contains approximately six acetyl groups per molecule. The infrared absorption spectra and nuclear magnetic resonance spectra of the tri-' and hexa-acetyl products indicate that they are 0- acetyl derivatives. However, when the antibiotic is reacted with acetic anhydride in pyridine at the reflux temperature, a mixture of O-acetyl and N-acetyl products results. The U.V. spectrum of the lattera'cetylated product shows absorption characteristics of an N- acetyladenine.

The antibiotic forms pharmaceutically acceptable salts with suitable inorganic acids such hydrochloric acid, sulfuric acid, phosphoric acid arid the like; and with suitable organic acids such as 'maleic, tartaric, acetic, propionic, succinic, citric, methanesulfonic, naphthalenesulfonic and the like. A9l45 also forms a bright yellow picrate which melts at about l60-l62 C. after crystallization from hot water.

7' Addition of a saturated aqueous solution of piifiwa'r'x ray diffraction pattern of the p-hydroxyazobenzene sulfonate salt of A-9145, using vanadium filtered chromium radiation and a wave-length value of 2.2896 A for calculating the interplanar spacings, gives the following intensity values:

The behavior of antibiotic A-9-l45 on a number of paper chromatograms employing different solvent sys-' tems for development isshown below in Table I. Whatman No. 1 paper was employed except where otherwise indicated. The loaction of the antibiotic following development of the chromatogram was determined by a bioautograph with the organism Saccharomyces pas- -torianus.

TABLE L-PAPE R OIIROMAAIO GRAPHY OF ANTIBOBIOTIC Solvent system man N o. 4 paperimpregnated with 1N sodium sulfate bufier .07 Mcthanol:0.1 N hydrochloric-acid (3:1) .47 Ten percent aqueous propanol .09 Methanol: .05 M sodium citrate at pH 5.7 (70:30) with paper buifcrcd with .05 M sodium citrate at pH 6.7 .34

1 Bl value is the ratio of the distance traveled by the antibiotic from the origin to the distance traveled by the solvent front from the origin.

Stability studies carried out on substantially pure an tibiotic A-9145 in aqueous solution over the pH range from pH 3 to pH 9 at a temperature of about 25 C. showed no decomposition and little loss in activity.

The free base of antibiotic A-91'45 has an inhibitory action against the growth of microbial organisms, both bacteria and fugi, which are pathogenic to animal and plant life. it is particularly effective in inhibiting the growth of pathogenic fungi both in vitro and in vivo. For example, the minimum inhibitory concentration of A-914S expressed in mcg./ml., as determined in the standard agar dilution test, for three illustrative organisms is as follows: Ceratostomella ulmi, 100; Helminthosporium sativum, 100; Penicillium expansum, 100. In the standard paper disc assay method a 100 mcg./ml. solution of A-9145 produced a 35 mm. zone and a 25 mm. zone of inhibition against Saccharomyces pasrorianus and Candida tropicalis, respectively.

The antibiotic is particularly inhibitory for the growth of the pathogenic fungus, Candida albicans. For example, the growth of Candida albicans in Sabourauds broth was inhibited 64 percent when the concentration of A-9145 was 0.019 meg/ml. The extent of growth inhibition was measured spectrophotometrically by determining the percent light transmittance at 660 my. compared to a control broth.

When administered orally or parenterall y to warm blooded mammals, antibiotic A-9145 is effective in combating systemic fungal infections. The in vivo antifungal activity of A-9145 is demonstrated by the following data obtained when A-9l45 was administered to mice infected with C7 albicans A-26. The data were obtained from tests carried out in the following manner. Two groups of mice, one a control group, were exposed to a sublethal dose of X-irradiation 24 hours prior to infection with C. albicans A-26. Infection was accomplished by the intravenous administration of 1.5 X 10 cells of C. albicans per mouse. The mice of the treatment group were administered anitbiotic A-9145 by various routes at O, 2, 24 and 26 hours post infection. The control group of mice received no antibiotic. The in vivo antifungal activity was determined by comparing the average survival time of the treatment group with the average survival time of the control group. Table II shows the results obtained in the above test.

"TABLE 11 Route of administration (mg/kg) 30 Subcutaneous 128 40 lntraperitoneal 10 Oral (gavage) 69 The total dose is the sum of the four equal doses administered at 0, 2, 24 and 26 hours post infection.

2 The Average Survival Time Beyond the Control group is the average survival time of the treated group of mice compared to the average survival time of the control group of mice expressed as a percentage. The average survival time of each group is the sum of the survival time of each mouse in the group divided by the total number of mice in the group.

The antibiotic A-9l45 is a relatively non-toxic substance having an LD of 184.9 1 l. 1.3 mg./kg. when injected subcutaneously in mice.

Antibiotic A-9145 is effective in combating systemic infections of C. albicans when administered orally or subcutaneously in a single dose of from about 20 mgl/kg. to about 100 mgJkg. If desired, a dose regimen comprising periodic administration of smaller doses, as, for example, a-dose'of about 1 -mg./kg.' to about 5 mg./kg. two'or three times daily; can be employed to obtain the desired antifungal effect.

The-antibiotic can be administered by the parenteral route'as an isotonic solution, as for example in isotonic saline. For oral administration the antibioticcan be suitably formulated as well known in the art, as, for example, in capsules, tablets, or as a suspension of an insoluble salt form.

Antibiotic A-9145 is also effective in combating the growth of organisms pathogenic to plant life. For example, the antibiotic is effective for the control of several pathogens causing disease states in economically important plants. Table 111 lists several illustrative diseases, and the causative organisms thereof against which A-9l45 demonstrates activity in the indicated test plant.

var. .rojensis In the case of foliar plant diseases such as powdery mildew, bean rust, anthracnose and bacterial blight, the antibiotic is preferably applied to the diseased plant as a foliar spray by employing an aqueous spray solution of the antibiotic at a concentration of from about 50 to about 400 ppm. The aqueous spray solution desirably also contains a wetting agent to allow more even distribution of the antibiotic over the leaf surface. In the case of plant diseases such as crown galhdrench or spray of an'aqueous solution of the antibiotic at a concentration of from about 10 to about 200 ppm.,is applied to the locus of the infected plant.

Antibiotic A-9l45 is also effective in preventing the development of disease symptoms in plants exposed to the disease causing organism and treated prior to the development of disease symptoms.

The antibiotic A-9l45 is produced by culturing an A 9 producing strain of the organism Streptomyces .griseolus under submerged aerobic fermentation conditions in a nutrient medium containing assimilable sources of carbon, nitrogen and inorganic salts until a substantial level of antibiotic activity is obtained. The

antibiotic is isolated from 'the filtered fermentation broth, suitablyby chromatography over a cationic ex- S. griseolus are S. antibioticus and S. aureofaciena change resin of the [RC-50 type, and can be purified further, as for example by chromatography over a nonionic type adsorbent such as carbon.

The A-9l45 producing organism was isolated from a soil sample acquired from the Ivory Coast region of the continent of Africa and can be obtained from the culture collection maintained by the UnitedStates Department of Agriculture, Agricultural Research Service, Northern Utilization Research and Development Division located at 1815 North University Street, Peoria, Illinois 61604, where it is deposited without restriction as to public availability and has been assigned the accession number, NRRL 3739.

The organism has been classified as a strain of Streptomyces griseolus (Waksman), Waksman and Henrici, S. A. Waksman, 1961. The Actinomycetes, Vol. 2, Classification, Identification and Description of Genera and Species. The Williams and Wilkings Co., Baltimore, Md. Other species of Streptomyces similar to However, they are differentiated from the A-9l45 pro ducing microorganism in that S. antibioticus produces a melanin pigment and S. aureofaciens may produce spiral sporophores on some media and a soluble yellow pigment.

S. griseolus NRRL 3739 produces long flexuous sporophores and short cylindrical spores which are yellow gray to gray en masse. The vegetativemycelium is yellow to grayish yellow. Although the vegetative mycelium may fragment in liquid culture media, a characteristic of the Nocardia species, cell wall analysis according to the procedure described by Becker et al. Appl. Microbiol. 12, 421-423 (1964) indicates the presence of only the L,L isomer of diaminopimelic acid, a characteristic of the Streptomyces genus. The A-9145 producing organism is assigned to the Rectus- Flexibilis Gray series of Pridham et al., Appl. Microbiol. 6, 52-79 (1958) and to the Gray series of the Tresner and Backus system, Appl. Microbiol. 11, 335-338 (1963).

The following paragraphs contain a description of the morphological and cultural characteristics of S. griseolus NRRL 3739. The methods recommended for the International Streptomyces Project for the characterization of Streptomyces species have been employed along with certain supplementary tests. Shirling and Gottlieb, Intern. Bull. Systematic Bacteriol., 16, 313-340 (1966). Color names were assigned according to the ISCC-NBS method, Kelly and Judd, The ISCC- NBS Method of Designating Colors and a Dictionary of Color Names. U.S. Dept. of Commerce Circ. 553 (1955), Washington, DC. Figures in parentheses refer to the-Tresner and Backus color series, op. cit., and color tab designations are underlined. The numbers and letters in brackets refer to the Maerz and Paul color blocks, Dictionary of Color, I955 McGraw-Hill Book Co., Inc., New York. Cultures were grown at a temperature of 30 C. for [4 days unless otherwise noted.

Cultural characteristics of S. griseolus NRRL 3739 -on various culture media:

agar

Growth Characteristics Abundant growth, reverse,

medium dark grayish yellow [1354]; aerial mycelium and rrporulation is abundant, light grayish reddish brown, (GY) Sfe [5C7]; no soluble pigment.

Good growth, reverse medium grayish yellow [20 Cl]; aerial mycelium and sporulation good, yellowish gray (GY) 2dc [27A1]; no soluble pigment.

Good growth, reverse medium,

moderate yellow, [1H2]; fair to good aerial mycelium and sporulation, light gray to white, (GY) d (W) b [35A2]; slight brown soluble pigment is produced.

Good growth, reverse medium, light yellow brown [13E6]; good aerial mycelium and sporulation, yellowish gray (GY) Zdc [12A3]; no soluble pigment produced.

Good growth, reverse medium,

oran e yellow [1H7]; scant aeri mycelium and sporulation, grayish "ellowish pink (R) Sec 111A4 no soluble pigment procuced.

Good growth, reverse medium, light grayish olive [HI-l4]; scant aerial mycelium and Culture Warm ICI No. 2 agar ICP No. 3 agar ICP No. 4 agar ICP No. 5 agar Bennett's agar Glycerol-Glycine medium, white [42A1]; poor aerial mycelium and sporulation prevented a color designation.

Good growth, reversemedium, grayish yellow 12B2]; no aerial mycelium or sporulation. A slight yellow pigment was observed.

Good growth, reverse medium, grayish yellow [12Cl]; no

Calcium malate agar Nutrient agar aerial mycelium or sporulation,

, I no soluble pigment Emerson's agar Abundant growth, reverse [1318]; scant aerial mycelium and sporulation; white (W) b 142A1]; no soluble pigment.

Tomato pasteoatmeal agar Abundant growth, reverse medium, light grayish olive [1515]; abundant aerial mycelium and sporulation; light gray (GY) d [44A2], also some white area (W) b; no soluble pigment.

Glucose Asparagine J Good growth, reverse medium grayish greenish yellow [12E2]; good aerial mycelium and sporulation, yellowish gray' (GY)'2dc [27A1]; no soluble pigment.

Good growth, reverse medium,

grayish greenish yellow [12E2]; good aerial mycelium and sporulation development; yellowish gray (GY)Zdc [27Al 1, no soluble pigment.

' International Styreptomyces Project medium Additional cultural characteristics:

Tyrosine agar Test Results Nitrate reduction positive Action on milk Coagulation at 14 days and slight clearing Complete at 14 days Gelatin liquefaction Llsdiaminopimelic acid only negative negative Results Growth from 26 to 37 C; no growth at about 43 C.

medium strong yellowish brown Stab culture for oxygen No growth below surface;

aerobic. requirement on lCP Table IV contains the observed results of experiments carried out to determine the carbon utilization characteristics of S. griseolus NRRL 3739.

TABLE IV Carbon Utilization by S. griseolus NRRL 3739 Utilization PREPARATION OF A-9l45 The A-9l45 producing organism, S. griseolus NRRL 3739, was isolated from the soil sample by serial dilution and transferred to a nutrient agar slant for culturing. In producing the antibiotic, a small amount of growth on the agar slant is transferred with a sterile platinum loop to a vegetative culture medium. The inoculated vegetative medium is then incubated until substantial growth develops. The cultured vegetative medium is employed a the inoculum for the production medium. It is preferable to employ the growing vegetative medium as the inoculum for the production me dium rather than spores from the agar slants because, when a spore inoculum is used, a considerable time lag is observed prior to antibiotic production during the fermentation. The cultured vegetative medium, on the other hand, is a viable growing culture of the organism and its use as inoculum results in a shorter start up time for the production fermentation.

The A-9l45 producing organism S. grisealus NRRL 3739 can be grown in any one of a number of nutrient media containing assimilable sources of carbon, nitrogen and inorganic salts. Carbon sources such as the carbohydrates sucrose, fructose and glucose can be employed; however, for economy of production molasses is a desirable carbohydrate source. Nitrogen sources which are suitable media ingredients include com steep, soybean meal, peptones, casein hydrolysates, distillers solubles, casein, amino acid mixtures, and the like. Inorganic salts which can be employed as nutrient constitutents include the usual salts capable of yielding sodium, ammonium, potassium, calcium, chloride, phosphate, sulfate, acetate, carbonate and like ions. Additionally, various essential trace elements should also be included in the culture medium for the growth of the A-9l45 producing organism of this invention. Such trace essential elements are usually supplied as impurities along with other medium constituents. Sources of growth enhancing factors such as yeast'extracts and beef extracts can also be included in the mediua.

The A-9l45 producing organism Sfgriseolus NRRL 3739 can be grown under varying conditions of temperature and pH. For example, the organism will grow over the pH range of from about pH 6.0 to about pH 8.5. However, prior to inoculation with the organism, it is preferable to adjust the pH of the culture medium to between about pH 6.0 and pH 7.5. As is commonly observed with other actinomycetes, the pH of the fermentation medium gradually increases and may reach a value of from about pH 8.0 to about pH 8.5 during the production of A-9145.

The organism can be grown well at temperatures between about 26+ C. and about 35 C.'The preferred temperature range for optimal production of the antibiotic appears to be about 28 C. to about 32 C.

For large scale production of A-9145, submerged aerobic fermentation in large fermentors is employed.

smaller quantities of the antibiotic are obtained conveniently by shake flask fermentations of from one-liter to 25-liter capacity.

In carrying out the A-9l45 fermentation by sub merged aerobic fermentation, sterile air is blown through the agitated culture medium. For efficient growth of the organism and production of the antibi otic, the volume of sterile air blown through the medium in large tank fermentations is upwards of 0.2 volume of air per volume of culture medium per minute. More efficient growth of the organism and antibiotic production is obtained whenthe volume ofair employed is about 0.5 volume of air per volume of culture medium per minute.

The progress of the fermentation and the level of antibiotic acitivity in the culture medium can be followed during the growth period by testing samples of the cul-' ture medium for their antibiotic activity against organisms known to be sensitive to the antibiotic. One such organism is Sqccharomyces pastorianus ATCC 2366. The bioassay can be carried out by standard assay procedures, for example, the turbidimetric method or the paper disc assay method. In general, maximum production of the antibiotic occurs within about two to five days when submerged aerobic fermentationis carried out in large tanks or shake flasks.-

Antibiotic A-9l45 can be recovered from the fermentation medium by employing extractive and adsorptive techniques. Adsorptive techniques are prefer able to extraction procedures because the latter generally require the use of large volumes of solvents.

Cationic exchange resins, such as the resins of the polystyrenesulfonic acid and methacrylic carboxylic acid type, for example, IRC-SO can be employed as adsorbents for the recovery and isolation of antibiotic A-9l45.

The A-9145 containing fermentation medium is first filtered to remove the mycelium. The useof a filter acid such as kieselguhr is desirably employed in the filtration. The filtered broth is then passed over a cationic exchange resin, preferably lRC-50 in the hydrogen cycle, and the resin containing the adsorbed antibiotic is washed with water to remove impurities. The antibiotic is then eluted from the resin with dilute mineral acid. The preferred acid is sulfuric acid at a normality of about 0.05 N. The eluate fractions containing antibiotic activity are combined and neutralized by the addition of base, such as an alkali metal hydroxide or an alkaline earth metal hydroxide. Barium hydroxide is the preferred base because the neutralized sulfuric acid precipitates as the insoluble barium salt and is easily removed from the eluate by filtration.

The antibiotic is recovered from the neutralized eluate as the free base by concentration of the eluate in vacuo to a low volume. Upon theadditionof a water soluble. organic solvent, such as methanol, ethanol or acetone the antibiotic A-9l45 precipitates as a solid and is collected by filtration.

The antibiotic preparation thus obtained can be further purified; however, for some purposes it may be de-' sirable for economic reasons to emoloy the antibiotic without further purification.

The antibiotic acn be further purified by chromatography over any of a'number of non-ionic adsorbent materials such as activated carbon, cellulose, dextran, silica gel, and alumina. The antibiotic is preferably obtained in a substantially pure state by successive chromatography over carbon, microcellulose and dextran adsorbents or alternatively over carbon followed by chromatography over Dowex 50 (NR A preferred adsorbent is carbon and the antibiotic is preferably eluted from the carbon with acetonezwater (3:7 v/v). The prferred cellul ose:adsorbent is a microcellulose. The antibiotic is eluted from the cellulose with acetonitrilezwater (1:1, v:v). ln the final purification step, the antibiotic A-9145 obtained from the column is option ally washed with water through a column or filter packed with dextran to remove any remaining inorganic impurities which may be present. The active factions are combined and concentrated to a small volume. A water miscible organic solvent such as methanol is added to the antibiotic aqueous concentrate to form a solid precipitate of A-9l45 in its substantially purestate.

The present invention is further illustrated-by the following specific examples.

EXAMPLE 1 Spores of streptomyces griseolus strain NRRL 3739 are inoculated on a nutrient agar slant having the following composition:

lngredient Weight (g.) Dextrin -10 Casein hydrolysates 2 Beef extract 1 Yeast extract I Agar Water (0.8. to a volume of one liter) Pancreatic hydrolysate of casein. (N-Z Amine A Sheffield Chemical Co., Norwich, N.Y.)

The slant is incubated for 5 days at a temperature of 30 C. The mature slant culture is covered with a small amount of sterile distilled water and is scraped gently to loosen the spores.

One ml. of the resulting spore suspension is used to inoculate l00 ml. of a sterile vegetative growth medium having the following composition:

Ingredient Weight (g.) Glucose l5 Soybean meal [5 Corn steep solid: 5 Calcium carbonate 3 2 Sodium chloride 5 Water, q.s. to make one liter The percentages shown are expressed on a weight-pervolume basis:

Ingredient Glucose Dextrin Soybean meal (grits) Edible molasses Brewers Yeast Extract Calcium carbonate added to a volume of 25 liters.

Amber BYF 300, Amber Laboratories, Juneau, Wisconsin.

The inoculated culture medium contained in a 30-liter fermentation tank is allowed to ferment at a temperature of about 30C. Throughout the fermentation period the medium is stirred and aerated with sterile air in an amount of about one-half vome of air per volume of culture medium per minute. The fermentation is allowed to continue for about 3 days, during which time the culture medium gradually increases in pH from an initial level of about pH 6.5 to about pH 7.3.

liters of fermentation broth thus obtained is 'filtered in vacuo with the aid of 2 percent l -lyflo supepcel filter aid to remove the mycelium. The filtered broth containing the antibiotic A-9l45 is passed over a column measuring TX cm. containing the cationic exchange resin [RC- 50 in the hydrogen cycle. The column is washed with ten liters of water and the washings are discarded.

The column containing the adsorbed A-91'45 is eluted with 30 litersjof 0.05 N sulfuric acid. The eluate is neutralized with a saturated solution of barium hydroxide and the precipitate of barium sulfate is filtered. The'filtrate is concentrated in vacuo to a volume of about 100 ml., is then filtered to remove solid impurities and is added to about 2,000 ml. of methanol. The antibiotic precipitates and is filtered and dried in vacuo to yield about 4.5 g. of crude antibiotic A3145, The

crude A-9l45 so obtained is dissolved in 100 mlyof water and passed over a columm measuring 2 X 70 cm. containing Pittsburgh 12 X 40 carbon. The column is washed with 400 ml. of water until a clear colorless wash is obtained. The antibiotic is eluted from the carbon with acetonezwater (3:7). The antibiotic containing eluate is concentrated in vacuo to a volume of about 100 ml. and the concentrate is added to 2 liters of methanol. The antibiotic precipitates and is filtered and dried in vacuo to yield about 2 g. of A-9145.

Two grams of the antibiotic so obtained are dissolved in about 20 ml. of water and the solution is passed over a column measuring 4.7 X 60 cm. containing microcellulose adsorbent sold commercially under the designation Avicel (FMC Corporation, Newark, N.J.). The adsorbent is.packed into the column with acetonitrilezwater (7:3). The column containing the adsorbed antibiotic is washed successively with two liters each of acetonitrilezwater (7:3) and (6.5:3.5). The column is then eluted with acetonitrile:- water (1:1) and the-antibiotic containing eluate is concentrated to a volume of about 30 ml The concentrate is diluted with about 60 m]. of methanol and then poured into about 1,800 ml. of dry acetone to precipitate the antibiotic. The precipitate is filtered and dried to yield about 700 mg. of antibiotic A-9l45.

Antibiotic A-9l45 so obtained is further purified in the following manner: 700 mg. of A-9l45 is dissolved in about 25 ml. of water and passed over a column measuring 5.5 X 100 cm. containing Sephadex G-50 (coarse grade). The column is washed with water and acetonitrile:water the aqueous eluate containing the antibiotic is concentrated to a volume of about 20 ml. The concentrate is diluted with 60 ml. of methanol and is poured into about 1,600 ml. of dry acetone to precipitate the antibiotic. The A-9145 is filtered and dried in vacuo to yield about 530 mg. of white amorphous A-9l45 antibiotic powder.

EXAMPLE 2 Acid addition salts of A-9145 are prepared by treating an aqueous solution of the antibiotic, containing a water miscible organic solvent such as methanol, with an equivalent amount of the desired acid in a suitable solvent. The desired salt precipitates directly or upon addition or a water miscible organic solvent such as acetone. The following paragraphs illustrate the preparation of several salts of A-9145.

One hundred milligrams of A-9145 is dissolved in 1 ml. of water and 2 ml. of methanol are added to the solution. The pH of the solution is adjusted to pH 3.8 with 1N hydrochloric acid. Two milliliters of methanol are added to the acidic solution which is then poured into 100 ml. of acetone to precipitate the hydrochloride salt of A-9145. The hydrochloride metls at about 195197 C. after recrystallization from ethanolwater. Elemental analysis for chlorine: 8.17 percent.

To a solution of 100 mg. of A-9145 in 1 ml. ofwater, is' added 2 ml. of methanol and the pH of the solution is adjusted to about pH 4.0 with 1 N sulfuric acid. The addition of 3 ml. of water is necessary to maintain solution during the acid addition. The acidic solution is then added to about 120 ml. of methanol to precipitate the sulfate salt of A-9145. The sulfate salt is recrystallized from water-ethanol and melts after recrystallization at about 220-222 C. Elemental analysis for sulfur; 4.23 percent.

To a solution of 100 mg. of antibiotic A-9145 in 5 ml. of water is added ml. of a saturated aqueous solution of p-hydroxyazobenzenesulfonic acid. The bright orange p-hydroxyazobenzenesulfonate salt of A-9145 precipitates and is separated by centrifuge. The salt is recrystallized from hot water and melts at about 220222 C. Elemental analysis for sulfur: 6.92 percent.

We claim:

1. The antibiotic A-9145 or an acid addition salt thereof, said antibiotic being a white, solid, basic substancewhich is highly soluble in water and is substantially insoluble in methanol, ethanol, propanol and acetone; has the approximate elemental composition of 46.47 percent carbon, 6.8 percent hydrogen, 22.28 percent nitrogen and 26.22 percent oxygen; has four tritratable groups having pKa values of 2.9, 3.9, 8.9,-

neutral p ll 206 mu, E, 520

258 mp, E 325 acidic pH 256 mp, E, i 325 basic pH i I 2. A method of producing the antibiotic A-9145 as defined in claim 1 which comprises cultivating Strepmmyces griseolus NRRL 3739 in an aqueousculture medium containing assimilable sources of carbon, nitrogen and inorganic salts, under submerged aerobic conditions until a substantial amount of antibiotic activity is produced by said organism in said culture medium.

3. A method of producing the antibiotic A 9145 as defined in claim 1 which comprises cultivating Streptomyces griseolus NRRL 3739 in an aqueous culture medium containing assimilable sources of carbon, nitrogen and inorganic salts, under submerged aerobic conditions until a substantial amount of antibiotic activity is produced by said organism in said culture medium,-and recovering the A-9l45 from said culture medium. 

2. A method of producing the antibiotic A-9145 as defined in claim 1 which comprises cultivating Streptomyces griseolus NRRL 3739 in an aqueous culture medium containing assimilable sources of carbon, nitrogen and inorganic salts, under submerged aerobic conditions until a substantial amount of antibiotic activity is produced by said organism in said culture medium.
 3. A method of producing the antibiotic A 9145 as defined in claim 1 which comprises cultivating Streptomyces griseolus NRRL 3739 in an aqueous culture medium containing assimilable sources of carbon, nitrogen and inorganic salts, under submerged aerobic conditions until a substantial amount of antibiotic activity is produced by said organism in said culture medium, and recovering the A-9145 from said culture medium. 